Inhibition of rat microsomal lipid peroxidation by the oral administration of D002

• Published in: Brazilian journal of medical and biological research Vol. 33; no. 1; pp. 85 - 90
• Main Authors: Menéndez, R, Amor, A M, González, R M, Jiménez, S, Más, R
• Format: Journal Article
• Language: English
• Published: Brazil Associação Brasileira de Divulgação Científica 01.01.2000
• Subjects: Administration, Oral; Animals; Anti-Ulcer Agents - administration & dosage; Anti-Ulcer Agents - pharmacology; BIOLOGY; Brain - metabolism; Brain - ultrastructure; D002; Fatty Alcohols - administration & dosage; Fatty Alcohols - pharmacology; higher aliphatic alcohols; Lipid Peroxidation - drug effects; lipids; Male; MEDICINE, RESEARCH & EXPERIMENTAL; microsomes; Microsomes - drug effects; Microsomes - metabolism; Microsomes, Liver - drug effects; Microsomes, Liver - metabolism; peroxidation; Rats; Rats, Wistar; Thiobarbituric Acid Reactive Substances - analysis; D002; lipids; peroxidation; higher aliphatic alcohols; microsomes
• ISSN: 0100-879X; 1414-431X; 0100-879X; 0034-7310
• DOI: 10.1590/s0100-879x2000000100012

The effect of D002, a defined mixture of higher primary alcohols purified from bee wax, on in vivo and in vitro lipid peroxidation was studied. The extent of lipid peroxidation was measured on the basis of the levels of thiobarbituric acid reactive substances (TBARS). When D002 (5-100 mg/kg body weight) was administered orally to rats for two weeks, a partial inhibition of the in vitro enzymatic and non-enzymatic lipid peroxidation was observed in liver and brain microsomes. Maximal protection (46%) occurred at a dose of 25 mg/kg. D002 behaved differently depending on both the presence of NADPH and the integrity of liver microsomes, which suggests that under conditions where microsomal metabolism was favored the protective effect of D002 was increased. D002 (25 mg/kg) also completely inhibited carbon tetrachloride- and toluene-induced in vivo lipid peroxidation in liver and brain. Also, D002 significantly lowered in a dose-dependent manner the basal level of TBARS in liver (19-40%) and brain (28-44%) microsomes. We conclude that the oral administration of D002 (5, 25 and 100 mg/kg) for two weeks protected rat liver and brain microsomes against microsomal lipid peroxidation in vitro and in vivo. Thus, D002 could be useful as a dietary natural antioxidant supplement. More studies are required before these data can be extrapolated to the recommendation for the use of D002 as a dietary antioxidant supplement for humans.